FDA Inspection 1182400 — Fersinsa GB, SA De CV

Fersinsa GB, SA De CV — FEI 3000538793

The FDA completed an inspection of Fersinsa GB, SA De CV on Sep 23, 2022 in Ramos Arizpe. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 23, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ramos Arizpe (Mexico)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.